Quality in Technology Transfer Projects

  • Product Id : FDB3511
  • Category : , , ,
  • Presenter :
  • Scheduled On : October 03 2022 11:00 am
  • Duration : 60 Minutes

Technology transfer in pharmaceuticals seems complex or simple based on who is looking at it. For site manufacturing team, it may be complex as they’ve to do go through a series of processes before they can term a transfer to be successful.

For transferring site or R&D it may be a simple activity as they aim to transfer the product. They might also find it complex depending upon the approach followed at receiving site.

In this webinar we will try elucidating the whole TT process in 3-4 sections. A logical understanding of these sections will help you and the organization to implement a successful product transfer strategy.

Areas Covered in the Session :

  • Approach to technology transfer
  • Conditions for the project to be successful
  • Role of transferring site
  • Role of receiving site
  • Role of management

Who Should Attend:

  • Quality Assurance Departments
  • Validation and Qualification Teams
  • Engineering Departments
  • Manufacturing Departments
  • Operations Departments
  • Maintenance Teams
  • Every Personnel responsible for Technology Transfer

FDB3511

Saurabh Joshi

Saurabh Joshi is renown for his contributions in executing robotics and automation projects for industry 4.0 transformation. He has been a keynote speaker and trainer in various life sciences forums and conferences, globally.

An industry professional with over 20 years hands on experience in Quality operations, Quality systems, Tech. transfer, Compliance, Validation and Qualifications; has successfully lead numerous regulatory inspections from USFDA, MHRA, WHO GMP (Geneva), HPRA for reputed organizations he has been a part of, such as, Cipla, Microlabs, Wockhardt, Sun Pharma to name a few. He has been an external Quality consultant with Merck specialties Pvt. Ltd. (A Merck KGaA, Darmstadt Germany company) guiding from shop floor at site to leading corporate level functions.

His consulting expertise includes, gap assessments and SOP preparation, regulatory inspections, QMS, technology transfer, Process Validation and equipment qualification, GMP, Data Integrity and Artificial Intelligence & Robotics.

He’s currently working with ValGenesis as Director-Industry solution. In his role he’s responsible for expanding customer outreach and demonstrate platform capabilities with ValGenesis’ solutions to life science companies.

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  • Login Information with Password to join the session, 24 hours prior to the webinar
  • Presentation Handout in .pdf format
  • Presentation from the Speaker
  • Feedback form
  • Certificate of Attendance
  • Recording access Information with Password to view the webinar, will be sent 24 hours after the completion of the Live webinar.
  • Presentation Handout in .pdf format
  • Certificate of Attendance